Opportunity summary
Score3.0Public score shown from the verified overall while the stale axis breakdown refreshesThis canonical paper page includes Commercialization Proof and Related Resources.
ARXIV:2603.14717 · PROTEIN GENERATION · SUBMITTED 02 APR · 02:30 UTC · FRESHNESS STALE
ARXIV:2603.14717PROTEIN GENERATIONSUBMITTED 02 APR · 02:30 UTCFRESHNESS STALEarXiv
A training-free method for generating protein sequences from small family alignments using stochastic attention.
Opportunity summary
Pain A training-free method for generating protein sequences from small family alignments using stochastic attention.
Evidence 0 refs | 0 sources | 17% coverage
Blocker Evidence unverified
A training-free method for generating protein sequences from small family alignments using stochastic attention. We propose stochastic attention (SA), a training-free sampler that treats the modern Hopfield energy over a protein alignment as a…
Most protein families have fewer than 100 known members, a regime where deep generative models overfit or collapse. We propose stochastic attention (SA), a training-free sampler that treats the modern Hopfield energy over a…
ScienceToStartup currently rates this 3.0/10 on the public viability pass. Controls confirm SA encodes correlated substitution patterns, not just per-position amino acid frequencies.
Protein Generation moved forward this cycle; last verified April 2026. Public score 3.0/10.
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Score3.0Public score shown from the verified overall while the stale axis breakdown refreshesAnalysis summary
A training-free method for generating protein sequences from small family alignments using stochastic attention.
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Paper Pack
10.48550/arXiv.2603.14717A training-free method for generating protein sequences from small family alignments using stochastic attention.
Abstract
Most protein families have fewer than 100 known members, a regime where deep generative models overfit or collapse. We propose stochastic attention (SA), a training-free sampler that treats the modern Hopfield energy over a protein alignment as a Boltzmann distribution and draws samples via Langevin dynamics. The score function is a closed-form softmax attention operation requiring no training, no pretraining data, and no GPU, with cost linear in alignment size. Across eight Pfam families, SA generates sequences with low amino acid compositional divergence, substantial novelty, and structural plausibility confirmed by ESMFold and AlphaFold2. Generated sequences fold more faithfully to canonical family structures than natural members in six of eight families. Against profile HMMs, EvoDiff, and the MSA Transformer, which produce sequences that drift far outside the family, SA maintains 51 to 66 percent identity while remaining novel, in seconds on a laptop. The critical temperature governing generation is predicted from PCA dimensionality alone, enabling fully automatic operation. Controls confirm SA encodes correlated substitution patterns, not just per-position amino acid frequencies.
Source availability
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Extraction status
Derived fallbackRead summaries are estimated from adjacent metadata, not verified extraction rows.
Proof status
unverified0 refs; 0 sources; 17% coverage.
What was readable
Derived fallback: Estimated from adjacent evidence; not verified from source.
Viability
Time to MVP
Commercial
Export
Preparing verified analysis
Dimensions overall score 3.0
PROBLEM
A training-free method for generating protein sequences from small family alignments using stochastic attention. We propose stochastic attention (SA), a training-free sampler that treats the modern Hopfield energy over a protein alignment as a Boltzmann distribution and draws sa...
METHOD
Most protein families have fewer than 100 known members, a regime where deep generative models overfit or collapse. We propose stochastic attention (SA), a training-free sampler that treats the modern Hopfield energy over a protein alignment as a Boltzmann distribution and draws...
RESULT
ScienceToStartup currently rates this 3.0/10 on the public viability pass. Controls confirm SA encodes correlated substitution patterns, not just per-position amino acid frequencies.
WHY NOW
Protein Generation moved forward this cycle; last verified April 2026. Public score 3.0/10.
Abstract-backed public claims while anchored extraction refreshes.
A training-free method for generating protein sequences from small family alignments using stochastic attention. We propose stochastic attention (SA), a training-free sampler that treats the modern Hopfield energy over a protein alignment as a Boltzmann distribution and draws samples via Langevin dynamics.
Abstract-backed fallback claim; anchored extraction has not materialized a public claim row yet.
partial
Most protein families have fewer than 100 known members, a regime where deep generative models overfit or collapse. We propose stochastic attention (SA), a training-free sampler that treats the modern Hopfield energy over a protein alignment as a Boltzmann distribution and draws samples via Langevin dynamics.
Abstract-backed fallback claim; anchored extraction has not materialized a public claim row yet.
partial
ScienceToStartup currently rates this 3.0/10 on the public viability pass. Controls confirm SA encodes correlated substitution patterns, not just per-position amino acid frequencies.
Abstract-backed fallback claim; anchored extraction has not materialized a public claim row yet.
partial
Protein Generation moved forward this cycle; last verified April 2026. Public score 3.0/10.
Abstract-backed fallback claim; anchored extraction has not materialized a public claim row yet.
partial
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Concepts
Methods
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A training-free method for generating protein sequences from small family alignments using stochastic attention.
Segment
Protein Generation
Adoption evidence
No public code link in the paper record yet
Commercial read
3.0/10 public viability
Direct
Adjacent
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CITED BY
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status
missing
reason
passport_row_missing
proof status
unverified
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No verified cost estimate
confidence low
next verification path
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Source missing: Build Passport payload.
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Evidence coverage
OpportunityKernel evidence_receipt
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stale
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Build readiness
BuildPassport EvidenceState
passport absent
stale
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Artifact maturity
GitHub and Hugging Face maturity payloads
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stale
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Technical feasibility
partial
Current read
Runnable path is not fully verified.
Evidence
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Gaps
Next test
Run minimal reproduction from the Build Passport prototype path.
Market urgency
missing
Current read
Buyer urgency is not verified from source.
Evidence
0 references, 0 sources, 17% evidence coverage.
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Collect buyer interview, deployment evidence, or cited demand signal.
Buyer clarity
missing
Current read
No budget owner is verified for this paper.
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Defensibility
missing
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Defensibility signals are missing.
Evidence
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Refresh defensibility bars with source receipts.
Integration burden
missing
Current read
No public implementation surface observed.
Evidence
No GitHub or Hugging Face payload attached.
Gaps
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Write integration checklist from prototype path and target workflow.
Capital intensity
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Current read
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Regulatory load
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Current read
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Evidence
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Classify regulatory flags before commercialization planning.
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Paper authors are not treated as operators without consent.
People
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Gaps
Next verification path
Prototype owner missing.
Build Passport does not name an implementer.
People
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Gaps
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Operator workflow not sourced.
No buyer or workflow interview attached.
People
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People
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Regulatory need unclassified.
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People
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Gaps
Next verification path
ARTIFACTS
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DEFENSIBILITY
Defensibility and confidence evidence pending.
WATCHTOWER
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FORESIGHT
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OPPORTUNITYKERNEL CHANGES SINCE LAST VIEW
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RELATED PAPER UPDATES
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TIMELINE
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BUZZ
Buzz trend pending.